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FDA 510(k)

電鋒 BRAHMS PCT,電鋒 BRAHMS PCT CalCheck 5

K 號:K160729 · 2016-06-13

決定日期2016-06-13
產品代碼PMT
諮詢委員會MI (請提供完整的描述文本,以便進行翻譯。)
決定相當於

器材摘要

Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5 is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2016-06-13 under 510(k) number K160729. The device is classified under product code PMT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5?

Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5 is a medical device that received FDA 510(k) clearance on 2016-06-13. The listed applicant is Roche Diagnostics. The 510(k) number is K160729.

When did Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5 receive FDA 510(k) clearance?

Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5 received FDA 510(k) clearance on 2016-06-13, under 510(k) number K160729.

Who is the listed applicant for Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5?

FDA 510(k) 記錄將羅氏醫學診斷列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5?

The FDA product code for Elecys BRAHMS PCT, Elecys BRAHMS PCT CalCheck 5 is PMT.

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其他以 Roche Diagnostics 為申請人之記錄

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相關器械(代碼:PMT)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

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